Canonical Allele Identifier: CA366933755

Gene: DNAH11

Linked Data

• MyVariant Identifiers: chr7:g.21675697T>A (hg19) ; chr7:g.21636079T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21636079T>A , CM000669.2:g.21636079T>A	GRCh38
NC_000007.13:g.21675697T>A , CM000669.1:g.21675697T>A	GRCh37
NC_000007.12:g.21642222T>A	NCBI36
NG_012886.2:g.97865T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.4709T>A MANE Select	ENSP00000475939.1:p.Val1570Glu
ENST00000328843.10:c.4724T>A	ENSP00000330671.7:p.Val1575Glu
ENST00000409508.7:c.4709T>A	ENSP00000475939.1:p.Val1570Glu
ENST00000620169.4:c.4724T>A	ENSP00000481693.1:p.Val1575Glu
NM_001277115.1:c.4709T>A	NP_001264044.1:p.Val1570Glu
NM_001277115.2:c.4709T>A MANE Select	NP_001264044.1:p.Val1570Glu